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Patrick F Chinnery

Showing results (141-150 of 473) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|August 19, 2007
Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystoniaFriedrich Asmus, Anita Devlin, Marita Munz, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 11, 2011
Charcot-Marie-Tooth disease in Northern EnglandCharlotte Foley, Ian Schofield, Gail Eglon, et al.
Parkinsonism & Related Disorders|February 7, 2006
Allelic variation of a functional polymorphism in the serotonin transporter gene and depression in Parkinson's diseaseDavid J Burn, Watcharee Tiangyou, Liesl M Allcock, et al.
Science Advances|March 7, 2025
Origin and cell type specificity of mitochondrial DNA mutations in <i>C9ORF72</i> ALS-FTLD human brain organoidsYu Nie, Kornélia Szebényi, Lea M D Wenger, et al.
Human Genetics|December 16, 2004
Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigreeNeil Howell, Iwona Kubacka, Sharon M Keers, et al.
Neuromuscular Disorders : NMD|January 22, 2004
A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysisRobert McFarland, Robert W Taylor, Patrick F Chinnery, et al.
Journal of the Neurological Sciences|October 15, 2005
Minimum prevalence of spinocerebellar ataxia 17 in the north east of EnglandKate Craig, Sharon M Keers, Timothy J Walls, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2013
Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6Lynn Rochester, Brook Galna, Sue Lord, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 9, 2002
Late-onset axial jerky dystonia due to the DYT1 deletionPatrick F Chinnery, Paul J Reading, Emma L McCarthy, et al.
Hepatology (Baltimore, Md.)|August 29, 2009
Human liver stem cells originate from the canals of HeringNimantha De Alwis, Gavin Hudson, Alastair D Burt, et al.
Pageof 48

Showing results (141-150 of 473) with videos related to

Sort By:
Pageof 48
Movement Disorders : Official Journal of the Movement Disorder Society|August 19, 2007
Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystoniaFriedrich Asmus, Anita Devlin, Marita Munz, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 11, 2011
Charcot-Marie-Tooth disease in Northern EnglandCharlotte Foley, Ian Schofield, Gail Eglon, et al.
Parkinsonism & Related Disorders|February 7, 2006
Allelic variation of a functional polymorphism in the serotonin transporter gene and depression in Parkinson's diseaseDavid J Burn, Watcharee Tiangyou, Liesl M Allcock, et al.
Science Advances|March 7, 2025
Origin and cell type specificity of mitochondrial DNA mutations in <i>C9ORF72</i> ALS-FTLD human brain organoidsYu Nie, Kornélia Szebényi, Lea M D Wenger, et al.
Human Genetics|December 16, 2004
Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigreeNeil Howell, Iwona Kubacka, Sharon M Keers, et al.
Neuromuscular Disorders : NMD|January 22, 2004
A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysisRobert McFarland, Robert W Taylor, Patrick F Chinnery, et al.
Journal of the Neurological Sciences|October 15, 2005
Minimum prevalence of spinocerebellar ataxia 17 in the north east of EnglandKate Craig, Sharon M Keers, Timothy J Walls, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2013
Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6Lynn Rochester, Brook Galna, Sue Lord, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 9, 2002
Late-onset axial jerky dystonia due to the DYT1 deletionPatrick F Chinnery, Paul J Reading, Emma L McCarthy, et al.
Hepatology (Baltimore, Md.)|August 29, 2009
Human liver stem cells originate from the canals of HeringNimantha De Alwis, Gavin Hudson, Alastair D Burt, et al.
Pageof 48